Canonical Allele Identifier: PA2829690268
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1432983
ClinVar RCV Id: RCV001982145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Val1348Ala
CA1395846
NM_007123.6:c.4043T>C